Ghent University Academic Bibliography

Accelerated adaptive laboratory evolution : a tool for evolutionary biotechnology

Luna Declerck (UGent) , Florent Bouchon (UGent) , Wouter Demeester (UGent) , Chiara Guidi (UGent) and Marjan De Mey (UGent)

(2026) BIOTECHNOLOGY ADVANCES. 86.

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Axonal Eif5a hypusination controls local translation and mitigates defects in FUS-ALS

Diana Piol, Bilal Khalil, Tessa Robberechts, Theo Killian, Maria Georgopoulou, Gabriele Partel, David Wouters, Nikolai Hecker, Paraskevi Tziortzouda, Yana Verresen, et al.

(2026) NATURE NEUROSCIENCE. 29. p.53-66

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Improved protein binder design using β-pairing targeted RFdiffusion

Isaac Sappington, Martin Toul (UGent) , David S. Lee, Stephanie A. Robinson, Inna Goreshnik, Clara Mccurdy, Tung Ching Chan, Nic Buchholz, Buwei Huang, Dionne Vafeados, et al.

(2026) NATURE COMMUNICATIONS. 17(1).

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EPS inhibitor treatment of Salmonella impacts evolution without selecting for resistance to biofilm inhibition

Mathieu Joos, Sybren Van Ginneken, Xabier Villanueva, Marie Dijkmans, Guglielmo A. Coppola, Camilo Andrés Pérez Romero, Thijs Vackier, Erik Van der Eycken (UGent) , Kathleen Marchal (UGent) , Bram Lories, et al.

(2025) NPJ BIOFILMS AND MICROBIOMES. 11(1).

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Aortic and arterial manifestations and clinical features in TGFB3-related heritable thoracic aortic disease : results from the Montalcino Aortic Consortium

Michelle Su-Anne Lim, Dong-Chuan Guo, Walter Velasco Torrez, Andrew Lai, Jonathan Schweber, Nikita Garg, Julie Fleischer, Catherine Boileau, Julie De Backer (UGent) , Artur Evangelista, et al.

(2025) JOURNAL OF MEDICAL GENETICS. 62(2). p.82-88

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Bi-allelic variants in three genes encoding distinct subunits of the vesicular AP-5 complex cause hereditary macular dystrophy

Karolina Kaminska, Francesca Cancellieri, Mathieu Quinodoz, Abigail R. Moye, Miriam Bauwens (UGent) , Siying Lin, Lucas Janeschitz-Kriegl, Tamar Hayman, Pilar Barberán-Martínez, Regina Schlaeger, et al.

(2025) AMERICAN JOURNAL OF HUMAN GENETICS. 112(4). p.808-828

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Elevated plasma complement factors in CRB1-associated inherited retinal dystrophies

Lude Moekotte, Joke H. de Boer, Sanne Hiddingh, Aafke de Ligt, Xuan-Thanh-An Nguyen, Carel B. Hoyng, Chris F. Inglehearn, Martin Mckibbin, Tina M. Lamey, Jennifer A. Thompson, et al.

(2025) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. 66(2).

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Characterising the refractive error in paediatric patients with congenital stationary night blindness : a multicentre study

Austin D. Igelman, Elizabeth White, Alaa Tayyib, Lesley Everett, Ajoy Vincent, Elise Heon, Christina Zeitz, Michel Michaelides, Omar A. Mahroo, Mohamed Katta, et al.

(2025) BRITISH JOURNAL OF OPHTHALMOLOGY. 109(2). p.286-292

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Preparedness, prevention and control related to zoonotic avian influenza

Julio Alvarez, Anette Boklund, Sabine Dippel, Fernanda Dorea, Jordi Figuerola, Mette S. Herskin, Virginie Michel, Miguel angel Miranda Chueca, Eleonora Nannoni, Soren Saxmose Nielsen, et al.

(2025) EFSA JOURNAL. 23(1).

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TFAP2E is implicated in central nervous system, orofacial and maxillofacial anomalies

Jeshurun C. Kalanithy, Enrico Mingardo, Jil D. Stegmann, Ramgopal Dhakar, Tikam Chand Dakal, Jill A. Rosenfeld, Wen-Hann Tan, Stephanie A. Coury, Audrey C. Woerner, Jessica Sebastian, et al.

(2025) JOURNAL OF MEDICAL GENETICS. 62(2). p.126-137

Academic Bibliography

Accelerated adaptive laboratory evolution : a tool for evolutionary biotechnology

Axonal Eif5a hypusination controls local translation and mitigates defects in FUS-ALS

Improved protein binder design using β-pairing targeted RFdiffusion

EPS inhibitor treatment of Salmonella impacts evolution without selecting for resistance to biofilm inhibition

Aortic and arterial manifestations and clinical features in TGFB3-related heritable thoracic aortic disease : results from the Montalcino Aortic Consortium

Bi-allelic variants in three genes encoding distinct subunits of the vesicular AP-5 complex cause hereditary macular dystrophy

Elevated plasma complement factors in CRB1-associated inherited retinal dystrophies

Characterising the refractive error in paediatric patients with congenital stationary night blindness : a multicentre study

Preparedness, prevention and control related to zoonotic avian influenza

TFAP2E is implicated in central nervous system, orofacial and maxillofacial anomalies

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